{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Hazelwood",
      "state": "MO",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70645",
      "recalling_firm": "Biomerieux Inc",
      "address_1": "595 Anglum Rd",
      "address_2": "N/A",
      "postal_code": "63042-2320",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution to United Kingdom and Turkey.  NO U.S. distribution.",
      "recall_number": "Z-1402-2015",
      "product_description": "Vitek 2 AST-P640 REF 418 579 Gram Positive Susceptibility Card, 20 cards per container, IVD.     Intended for use with the Vitek 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae.",
      "product_quantity": "2053 cartons",
      "reason_for_recall": "The outer carton label and package insert for the recalled product incorrectly lists Streptococcus pneumoniae as an organism for intended use.",
      "recall_initiation_date": "20150225",
      "center_classification_date": "20150408",
      "termination_date": "20170322",
      "report_date": "20150415",
      "code_info": "lot 740340920, expiration 14APR16;  lot 740350820, expiration 22JUL16;"
    }
  ]
}